The details of ternary fluoride crystallization in the system NaF-CaF<sub>2</sub>-AlF<sub>3</sub> have been specified. The phases NaCaAlF6, Na2Ca3Al2F14 and NaAlF4 have been obtained by high-temperature synthesis. Their thermal transformations have been studied using high-temperature X-ray diffraction. The occurring transformations can be considered in a quasibinary system CaF2-NaAlF4, where at T = 745°C - 750°C invariant equilibrium is established with the phases CaF<sub>2</sub>-NaCaAlF<sub>6</sub>-Na<sub>2</sub>Ca<sub>3</sub>Al<sub>2</sub>F<sub>14</sub>-(NaAlF<sub>4</sub>). The compounds NaCaAlF<sub>6</sub> and Na<sub>2</sub>Ca<sub>3</sub>Al<sub>2</sub>F<sub>14</sub> are stable in different temperature ranges. The phase NaCaAlF6 was fixed by rapid quenching from the melt. It decomposes at heating before 640°C yielding Na<sub>2</sub>Ca<sub>3</sub>Al<sub>2</sub>F<sub>14</sub> and NaAlF<sub>4</sub>. Direct and inverse transformations between NaCaAlF6</sub> and Na<sub>2</sub>Ca<sub>3</sub>Al<sub>2</sub>F<sub>14</sub> occur in the bulk samples of the electrolyte. A thermal treatment procedure was proposed for the solid electrolyte sample to get a sample corresponding to the composition of the melt and providing high phase crystallinity for the purposes of quantitative X-ray phase diffraction analysis.
Calcium fluoride combined with the excess of aluminum fluoride is the most widely used additive for decreasing the operation temperature in an electrolysis bath in aluminum production [
The quantitative phase determination in electrolytes containing calcium fluoride presents a methodological problem. In the course of the crystallization calcium fluoride forms three phases: CaF2 (fluorite), NaCaAlF6 and Na2Ca3Al2F14 (calcium cryolites). Since calcium fluoride is able to bind aluminum fluoride and sodium fluoride during the process of crystallization, it is necessary both to determine its chemical concentration and to measure the content of each calcium-containing phase (NaCaAlF6 and Na2Ca3Al2F14). It has been mentioned in literature that the correlation between the calcium phases changes depending both on the electrolyte composition and sampling procedure [3-5]. The phase NaCaAlF6 is very poorly crystallized, decreasing the accuracy of its measurement by the XRD method including the application of the Rietveld technique [
The first description of the phase relations in the system NaF-AlF3-CaF2 was published by Fedotyev and Ilyinsky in 1912 [
In this paper, the conditions for the ternary phase crystallization in the system NaF-CaF2-AlF3 have been specified. The individual phases NaCaAlF6, Na2Ca3Al2F14 and NaAlF4 have been synthesized. Their thermal transformations have been studied using high-temperature X-ray diffraction technique. A thermal treatment procedure for the solid electrolyte sample has been proposed to get a sample corresponding to the composition of the melt and providing high phase crystallinity for the purposes of quantitative X-ray phase diffraction analysis.
Individual crystal phases NaCaAlF6 and Na2Ca3Al2F14 were synthesized from stoichiometric mixtures of a chemical grade AlF3 (99%), NaF (99%) and CaF2 (98%) at high temperature solid-state sintering. The detailed description of the synthesis is presented in [
Three samples of a calcium-containing electrolyte with CR 1.9, 2.4, 2.7 and CaF2 concentration equal to 8% (mas.) labeled as E1, E2, E3 were synthesized from the mixtures of the fluorides AlF3, NaF, and CaF2. The 10 g fluoride mixture was loaded in a platinum crucible closed with a cap and melted in a furnace at about 960 to 1000˚C for 20 min depending on the CR value and then cooled in air.
X-ray diffraction patterns were scanned by an X’Pert Pro (Panalytical) diffractometer, equipped with a PIXel detector with a graphite monochromator. CuKα-radiation was used. The scans were made in the range from 10˚ to 80˚, with a step of 0.026˚ (2Q) and the total scanning time being 12 min. The samples were prepared by direct loading into a cuvette of 27 mm in diameter.
High temperature X-ray studies were carried out using an X’Pert Pro (Panalytical) Diffractometer with a high temperature chamber NТK1200N “Anton Paar” in vacuum. The sample was prepared in a platinum cuvette of 10 mm in diameter. The sample weight was about 200 mg. The temperature of the sample was increased and decreased at a rate of 50˚/min to a certain temperature and then an X-ray diffraction pattern was taken in the range from 5 to 80˚ (2Θ) for 5 min. Then, the process was repeated at the next temperature stage. The X-ray data were processed with the help of High Score Plus software (Panalytical) [
The presence of four and, sometimes, five phases in the electrolyte samples contradicts to the Gibbs’s phase rule and indicates the non-equilibrium conditions of their formation. The system peculiarity is the location of the ternary phases in the section of CaF2-NaAlF4. This allows one to confine the possible electrolyte composition field by the triangle CaF2-Na3AlF6-NaAlF4. The double fluoride phases Ca2AlF7 and CaAlF5 have never occurred in the electrolyte samples and it is a well-grounded argument for marking this triangle field.
It was experimentally found that the pure phase NaCaAlF6 could only be obtained at a temperature above 710˚C but lower than 740˚C (the melting temperature). The pure phase Na2Ca3Al2F14 was synthesized at 500˚C - 620˚C. The phases NaCaAlF6 and Na2Ca3Al2F14 were investigated by high-temperature X-ray diffraction in a multistage heating procedure in vacuum. The X-ray diffraction data for both compounds were obtained at 100˚C, 300˚C, 400˚C, 500˚C, 550˚C, 570˚C, 600˚C. Some of the X-ray
diffraction patterns for NaCaAlF6 are presented in
Below 400˚C the phase NaCaAlF6 undergoes structural transformation (α → β) without changing the composition. At 500˚C the decay begins followed by the appearance of peaks of Na2Ca3Al2F14 and CaF2 at the X-ray powder pattern.
The phase Na2Ca3Al2F14 appears to be stable in vacuum approximately up to 600˚C and then decomposes into two products: CaF2 and Na3AlF6, which were observed in the X-ray diffraction pattern (
The high-temperature experiments have demonstrated that calcium-containing phases have different temperature intervals of stability. The phase NaCaAlF6 is metastable in normal conditions. Its relaxation in the conditions of low pressure and the thin sample, which do not prevent diffusion, begins at 500˚C and follows into Na2Ca3Al2F14. No reverse transformation was observed under the experimental conditions. The observed conversion can be explained by engaging the volatile instable phase NaAlF4 according to the following equations:
3NaCaAlF6 → Na2Ca3Al2F14 + NaAlF4 (1)
Na2Ca3Al2F14 → 2NaAlF4 + 3CaF2 (2)
5NaAlF4 → Na5Al3F14 + 2AlF3 (3)
Na5Al3F14 → Na3AlF6 + 2NaAlF4 (4)
The most expected decay reaction was not observed experimentally:
Na2Ca3Al2F14 → 2NaCaAlF6 + CaF2 (5)
The calcinations of the bulk samples at atmospheric pressure confirm these transformations of the calciumcontaining phases.
Experimental evidence for the participation of NaAlF4 in the above processes was obtained by the calcinations of NaCaAlF6 in a flow of an inert gas. The experimental details are described in [
As it was obtained from the X-ray diffraction data the prepared electrolyte samples were composed from the following phases: Na3AlF6, Na5Al3F14, NaCaAlF6, Na2Ca3Al2F14, and CaF2. The phase NaCaAlF6, dominated in the sample E3 (CR > 2.6), and the phase Na2Ca3Al2F14—in the samples E1 and E2 (CR < 2.3).
The presence of two and sometimes three calcium containing phases in the sample is a consequence of nonequilibrium crystallization. The phase NaCaAlF6 does not completely transform into Na2Ca3Al2F14 and in normal conditions remains metastable. It explains the broadened peaks on the X-ray diffraction pattern due to the crystalline degradation. According to the phase diagram of the system NaF-AlF3-CaF2 proposed by Anufrieva with the co-authors [
This distinction can be the reason for NaCaAlF6 prevailing in the electrolyte samples with CR > 2.7. The transformation of NaCaAlF6 into Na2Ca3Al2F14 at cooling results in NaAlF4 yielding. The active volatile molecules of NaAlF4 interact with the components of the electrolyte, in particular, with Na3AlF6, giving chiolyte. The decay of NaCaAlF6 occurs in the samples with varying degrees of completeness. This explains the variation of the phase composition for the samples with the same chemical content. However, from the analytical point of view a definite relation between the phase and elemental content is considered as the basis for the accuracy and precision, especially in the technological control in aluminum production. One of the ways to get corresponddence between the phase and elemental analysis is to analyze thermodynamically stable phases in the sample. This is why the conditions of the thermal treatment by calcination in air were investigated in the temperature range from 560˚C to 710˚C.
It was found that the phase compositions of the samples thermally treated at a temperature of 710˚C, 610˚C, 560˚C were different. Thus, calcium ions in the sample E1, calcinated at 710˚C were preferably collected in NaCaAlF6. In the samples heated at 610˚C and 560˚C calcium ions were predominantly in Na2Ca3Al2F14 (
Since the treated samples were in the solid state, the formation of Na2Ca3Al2F14 below 600˚C can be interpreted as the decay described by Equation (1). The released phase NaAlF4 interacts with cryolite, Equation (4). The described results were repeated with the samples E2 and E3. Thus, the experiments show that a sample regardless of its CR can be transformed into the equilibrium state. The high phase crystallinity suitable for further quantitative X-ray diffraction analysis was another important effect.
The obtained results were tested using the samples of an industrial electrolyte. The milled samples were placed into an open crucible and calcinated in a furnace at temperatures of from 450˚C to 650˚C for a predetermined time. The experiments showed that after calcinations at temperatures below 600˚C, poorly crystallized NaCaAlF6 transformed into well-crystallized Na2Ca3Al2F14 (
samples without NaCaAlF6 at temperatures below 600˚C did not induce changes in the X-Ray powder pattern. There was no any significant variation mentioned of the elemental composition of the sample. Thus, the optimal temperature for the thermal treatment is about 600˚C. The calcination at a temperature above 600˚C results in the presence of NaCaAlF6.
It is found that the interconversion of ternary fluorides NaCaAlF6 and Na2Ca3Al2F14 occurs in the electrolyte samples at cooling. At sampling the non-equilibrium cooling conditions stops the phase transformation and results in poorly crystallized Ca-containing phases. An additional thermal treatment procedure can be applied to achieve good phase crystallinity without changing the elemental composition. The approach is effective when using XRD analysis for the electrolyte monitoring at aluminum production. The optimal temperature for the thermal treatment is about 600˚C which provides the complete transformation of NaCaAlF6 into Na2Ca3Al2F14.
The investigations were carried out with the financial suport of State contracts No. 14.516.11.0080 (01.06.2013) of the Ministry of Education and Science of Russia, RFBR Grants: 11-03-00610a.